Cyclotron
Cyclotron
Cyclotron
I.
A.
B.
HISTORY
Previous Accelerators
The Cyclotron was developed in the wake of the successful linear accelerator (linac), a particle accelerator
still used today due to its advantages over circular accelerators in the realm of heavy ion acceleration. The
motivation of the linac was to accelerate charged particles using a lower voltage than a Van De Graff generator.
It succeeded by using a series of charged tubes fed by an
RF source to vary the charge to reuse the same voltage
differential many times, thereby accelerating a charged
particle[6] through multiple electrode gaps. See figure 1.
Cyclotron Development
Also at Physics
[email protected]
Department,
University
of
Ottawa.;
The undertaking of transforming this concept into reality was seized by a graduate student named M. Stanley
Livingston. He produced the first working model of the
2
cyclotron at 4.5in in diameter with the ability to accelerate ions up to 80 000 eV [7].
II.
HARDWARE
The construction of a primitive cyclotron is a product of relatively few pieces. To construct a cyclotron we
will refer to original patent filings[5] to describe necessary
parts and their roles.
III.
A.
THEORY
Cyclotronic Frequency
qB =
m 2
r
T =
m
qB
2r
2m
2m
=
=
qB
qB
resonance =
qB
m
or equivalently
fresonance =
qB
2m
3
is the relativistic velocity, while
1
=p
1 2
is the Lorentz factor.
m = m0
is the corrected mass Therefore, with relativistic consideration, the cyclotron resonance frequency would be
f=
f0
m0
qB0
D.
B.
When discussing particle accelerators, the characteristic most often mentioned is the energy of the apparatus.
This energy is the kinetic energy KE of an outgoing particle. In a cyclotron, the KE varies according to charge
and the mass of the particle involved. We begin with the
maximum gyroradius rmax a particle can have within the
cyclotron.
rmax =
m
qB
KE =
C.
qBrmax
m
(qBr)2
m 2
=
2
2m
Magnetic Focusing
41
Electric Focusing
During the path of a charged particle about the cyclotron, it is necessary to ensure the particle stays in the
center plane. This is done in the acceleration regions between the dees. This focusing is done by two cylindrical electric lenses that run along the top and the bottom
of gap between the Dees. The equation governing the
magnitude of electrical focusing is described by Stanley
Livingston as
2
eV0 z
1 eV0 z
=
sin
cos2
E
2 E
k
4
IV.
A.
USES
Medical
The difference, as you can see, is that reactor radioisotopes generally lie above the line of stability. Therefore
their decay mode is often whereas accelerator isotopes tend to have + emission or electron capture. This
decay mode leads to applications in molecular imaging
due to its high specific activity. Today there are close
to 20 radioisotopes with medical applications that can
be produced by cyclotrons, amongst which more than a
third have half lives less than an hour and a half [10].
These short lived isotopes must be manufactured on
site so that research may be carried out prior to total
decay. The advent of low cost medical cyclotrons has
the ability to revolutionize isotope research due to its
new found viability. Furthermore, as seen in the past 4
years with the Chalk River reactor, relying on a single
large source for isotopes such as Technetium 99 can be
disastrous for the medical community[4].
V.
NOTABLE EXAMPLES[1]
VI.
CONCLUSION
The cyclotron, while being a simple device by modern standards, is arguably the first generation of modern
particle accelerators. The energies obtained allowed the
us to examine the nucleus using particle bombardment,
allowed us to create new isotopes of medical importance
and create nuclear weapons. The fact that cyclotrons
are still used today is a testament to their simple and
versatile nature. While outclassed in modern physics by
CERN scaled accelerators, with the ability for more research hospitals to experiment with previously exotic radioisotopes, it is likely we will see many more advancements from the cyclotron in the applied domain.
[3] M. Stanley Livingston. The cyclotron. i. Journal of Applied Physics, 15(1), 1944.
[4] Tim Lougheed. Cyclotron production of medical isotopes
scales up. Canadian Medical Association Journal, 947,
2013.
B.
Manhattan
5
[5] L.E. O. Method and apparatus for the acceleration of
ions, February 20 1934. US Patent 1,948,384.
[6] American Institute of Physics. Early particle accelerators, 2014.
[7] APS Physics. Ernest lawrence and m. stanley livingston,
2014.
[10] M. A. AvilaRodr
guez, A. Z
arateMorales, and A. FloresMoreno. Cyclotron production of medical radioisotopes.
AIP Conference Proceedings, 1265(1), 2010.